# Study on the Mechanism of Neurodevelopment Dysplasia of Fetal Brain Caused by ASNS Gene Mutation

> **NCT03587155** · — · UNKNOWN · sponsor: **The First Hospital of Jilin University** · enrollment: 10 (estimated)

## Conditions studied

- Asparagine Synthetase Deficiency
- Genetic Diseases, Inborn

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT03587155
- **Lead sponsor:** The First Hospital of Jilin University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2017-10-28
- **Primary completion:** 2018-12
- **Final completion:** 2020-12
- **Target enrollment:** 10 (ESTIMATED)
- **Last updated:** 2018-07-16

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03587155

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03587155, "Study on the Mechanism of Neurodevelopment Dysplasia of Fetal Brain Caused by ASNS Gene Mutation". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT03587155. Licensed CC0.

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